A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414541



Internal ID21072094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120902920..121023267hg38UCSC Ensembl
chr5:120238615..120358962hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38120348
hg19120348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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